A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589866



Internal ID21781909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45986663..45988115hg38UCSC Ensembl
chr10:51607720..51609171hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381453
hg191452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008535
Supporting Variants
Samples
Known GenesTIMM23
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589866
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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